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Analyte sensors having a signal-to-noise ratio substantially unaffected by non-constant noise

a technology of analyte sensor and non-constant noise, applied in the field of analyte sensor, can solve the problems of likely diabetic behavior, inhibiting the ability of diabetics to make educated insulin therapy decisions

Inactive Publication Date: 2020-02-06
DEXCOM
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent describes an electrochemical analyte sensor that can be inserted into a host to measure the concentration of a specific analyte. The sensor has a membrane system that helps to reduce the effects of non-constant noise-causing electroactive species formed in the host. The membrane system can also include a torturous diffusion path or a resistance domain to further reduce the impact of non-constant noise-causing electroactive species. The sensor is designed to provide a signal that is at least about 80% of the signal over a time period of at least one day. Overall, the sensor has improved accuracy and reduced noise, allowing for accurate analyte concentration measurements in the host.

Problems solved by technology

In the diabetic state, the victim suffers from high blood sugar, which may cause an array of physiological derangements (for example, kidney failure, skin ulcers, or bleeding into the vitreous of the eye) associated with the deterioration of small blood vessels.
Conventionally, a diabetic person carries a self-monitoring blood glucose (SMBG) monitor, which typically comprises uncomfortable finger pricking methods.
Unfortunately, these time intervals are so far spread apart that the diabetic will likely find out too late, sometimes incurring dangerous side effects, of a hyperglycemic or hypoglycemic condition.
In fact, it is not only unlikely that a diabetic will take a timely SMBG value, but the diabetic will not know if their blood glucose value is going up (higher) or down (lower) based on conventional methods, inhibiting their ability to make educated insulin therapy decisions.

Method used

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  • Analyte sensors having a signal-to-noise ratio substantially unaffected by non-constant noise
  • Analyte sensors having a signal-to-noise ratio substantially unaffected by non-constant noise
  • Analyte sensors having a signal-to-noise ratio substantially unaffected by non-constant noise

Examples

Experimental program
Comparison scheme
Effect test

example 1

Resistance Domain Configurations to Increased the Analyte Signal Reduce Non-Constant Noise

[0412]Transcutaneous sensors, with electrode, interference, enzyme and resistance (polyurethane blend) domains, were built and tested in non-diabetic hosts. The control and test sensors were built as described in U.S. Publication No. 2006-0020187, which is incorporated herein by reference in its entirety, with the following exception: the resistance domain of the test sensors was formed of 3 layers of a 60% ChronoThane® H (CardioTech International, Wilmington, Mass., USA; the PEO concentration of ChronoThane® H is about 25%) polyurethane blend solution, as compared to a single layer of a 45% ChronoThane® H polyurethane blend solution in the control sensors. Test and control sensors were implanted bilaterally in the abdomens of non-diabetic host volunteers, for a period of about 7 days.

[0413]FIG. 8 illustrates exemplary test results from one test sensor, over a period of about 7 days, after sens...

example 2

A Lubricious Coating Configured to Reduce Non-Constant Noise

[0416]Control and test sensors, with electrode, enzyme and resistance domains, were built as described in U.S. Patent Publication No. US-2006-0020187-A1, including a resistance domain formed using a polyurethane polymer blend having about 8 wt. % PEO, as described in the section entitled “Polyurethane Polymer Material” above. A lubricious coating was applied to the test sensors by dipping them one time into a solution of HydroMed™ (CardioTech International, Inc., Wilmington, Mass., USA) and drying. The control and test sensors were tested in vitro (see Table 1, below). The test sensors (with the lubricious coating) had a substantially increased sensitivity (m) but with no corresponding increase in constant noise (b), when compared to control sensors (no lubricious coating). Accordingly, it was shown that application of a lubricious coating over a polyurethane blend resistance domain of a glucose sensor can (in vitro) substa...

example 3

Discontinuous Hydrophilic Overcoat on Resistance Domain Configured to Reduce Non-Constant Noise

[0418]To determine if a hydrophilic overcoat on the resistance layer can increase the analyte signal component and / or reduce the non-constant noise component, test and control sensors were build and tested in volunteer human hosts, over a period of 3 days. Both the test and control sensors included an electrode layer, an enzyme layer and a polyurethane blend resistance domain. The polyurethane blend used to form the resistance domain included 8% hydrophile (i.e., PEO). After fabrication, the test sensors were sprayed (one time) in a solution of 5% ChronoThane® H (about 25% PEO; CardioTech International, Wilmington, Mass., USA) and cured. Test and control sensors were implanted bilaterally in the abdomens of the volunteer human hosts. FIG. 10 is a graph showing test results from one exemplary sensor. Components of the Total Signal 1000 were determined, as described in Example 1. The Y-axis ...

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PUM

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Abstract

Systems and methods of use involving sensors having a signal-to-noise ratio that is substantially unaffected by non-constant noise are provided for continuous analyte measurement in a host. In some embodiments, a continuous analyte measurement system is configured to be wholly, transcutaneously, intravascularly or extracorporeally implanted.

Description

INCORPORATION BY REFERENCE TO RELATED APPLICATIONS[0001]Any and all priority claims identified in the Application Data Sheet, or any correction thereto, are hereby incorporated by reference under 37 CFR 1.57. This application is a continuation of U.S. application Ser. No. 16 / 453,925, filed Jun. 26, 2019, which is a continuation of U.S. application Ser. No. 14 / 145,404, filed Dec. 31, 2013, now U.S. Pat. No. 10,376,143, which is a continuation of Ser. No. 13 / 732,848, filed Jan. 2, 2013, now U.S. Pat. No. 9,763,609, which is a continuation of U.S. patent application Ser. No. 11 / 750,907, filed May 18, 2007, now U.S. Pat. No. 8,364,229. Each of the aforementioned applications is incorporated by reference herein in its entirety, and each is hereby expressly made a part of this specification.FIELD OF THE INVENTION[0002]The preferred embodiments relate generally to implantable devices, such as analyte sensors, and methods for detecting and / or measuring an analyte in a sample, such as a bodi...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61B5/00A61B5/1486A61B5/1473A61B5/145
CPCA61B5/14546A61B5/00A61B5/1473A61B5/14865A61B5/1486A61B5/14532A61B5/14735A61B5/6848A61B5/7203
Inventor SIMPSON, PETER C.BOOCK, ROBERT J.BRISTER, MARK C.RIXMAN, MONICA A.WOO, KUM MINGNGUYEN, LISABRUNNER, SETH R.CHEE, ARTHURNICHOLAS, MELISSA A.WIGHTLIN, MATTHEW D.PRYOR, JACKMARKOVIC, DUBRAVKA
Owner DEXCOM
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